Report shows Pfizer knew in January its mRNA jab was killing thousands, damaging three times more women than men
Smoking gun confidential Pfizer document exposes FDA criminal cover-up of VACCINE DEATHS… they knew the jab was killing people in early 2021… three times more WOMEN than MEN
Bypass censorship by sharing this link: https://www.afinalwarning.com/575723.html
Natural News) Thanks to the efforts of a group called Public Health and Medical Professionals for Transparency, we now have smoking gun confidential documents that show Pfizer and the FDA knew in early 2021 that pfizer’s mRNA vaccines were killing thousands of people and causing spontaneous abortions while damaging three times more women than men.
One confidential document in particular was part of a court-ordered release of FDA files that the FDA fought by claiming the agency should have 55 years to release this information. A court judge disagreed and ordered the release of 500 documents per month, and the very first batch of documents contained this bombshell entitled, “Cumulative Analysis of Post-Authorization Adverse Event Reports.”
The document reveals that within just 90 days after the EUA release of Pfizer’s mRNA vaccine, the company was already aware of voluntary adverse reaction reports that revealed 1,223 deaths and over 42,000 adverse reports describing a total of 158,893 adverse reactions. The reports originated from numerous countries, including the United States, United Kingdom, Italy, Germany, France, Portugal, Spain and other nations.
Aside from “general disorders,” the No. 1 most frequently reported category of mRNA vaccine adverse reactions was Nervous system disorders, clocking in at 25,957 reports.
Pfizer has withheld the total number of doses released across the world, citing corporate trade secrets. This is indicated by “(b) (4)” in the document, where specific numbers and facts are redacted.
Even these numbers — already quite shocking, given the FDA’s insistence that mRNA vaccines are “safe and effective” — barely scratch the surface of the damage and deaths caused by these vaccines. “Reports are submitted voluntarily, and the magnitude of underreporting is unknown,” says Pfizer on page 5.
Three times as many women damaged, compared to men
Shockingly, the document reveals that more than three times as many women were damaged by the Pfizer vaccine, compared to men. There were 29,914 adverse events recorded in women, with just 9,182 recorded in men. It is not known whether the same number of men and women took the vaccine, but this number exposes the very real possibility of a gender-specific vaccine damage risk that the FDA went to great lengths to cover up.
Anecdotally, most of the neurological damage we’ve seen in people who have been damaged by the vaccine — convulsions, numbness, pain, etc. — has been depicted in women, not men. It looks like the FDA knows the mRNA vaccine exhibits a disproportionate, gender-specific damage profile that also affects women in terms of spontaneous abortions (also covered in the report):
Pfizer told the FDA its mRNA covid vaccines can cause “enhanced disease” by making covid worse
Also to the shock of many observers who are just now digging into this smoking gun document, Pfizer told the FDA under “Safety concerns” (section 3.1.2) that its mRNA injection could cause, “Vaccine-Associated Enhanced Disease (VAED), including Vaccine-associated Enhanced Respiratory Disease (VAERD).”
This means the FDA knew the vaccine could sicken and kill patients who were later infected with covid.
Under the label of “missing information,” Pfizer also told the FDA that it has no information about “Use in Pregnancy and lactation” nor covering “Use in Paediatric Individuals < 12 Years of Age.”
“Vaccine Effectiveness” was also listead as “Missing information” by Pfizer.
In other words, Pfizer told the FDA its vaccines could kill people and that it had no information about vaccine effectiveness, yet the FDA fraudulently pushed the vaccine as “safe and effective” anyway. Pfizer even told the FDA that it had no safety information about use in pregnant women, yet the FDA (and Fauci, the CDC, etc.) all pushed the vaccine for pregnant women, despite the utter lack of safety information.
Based on this document, it appears that the FDA itself has been neck-deep in a criminal conspiracy to hide the truth about vaccine injuries and deaths while granting usage approvals to the very same corporations that openly told the FDA its products were killing people.
Note, too, that the entire corporate media complex has lied from day one, falsely claiming the vaccine has killed no one. They are, of course, complicit in this vaccine holocaust.
Spontaneous abortions, neonatal death and other effects on pregnant women
In the section labeled, “Use in Pregnancy and lactation,” the report discusses reports of the mRNA vaccine being linked to:
spontaneous abortion (23), outcome pending (5), premature birth with neonatal death, spontaneous abortion with intrauterine death (2 each), spontaneous abortion with neonatal death, and normal outcome (1 each).
Notice that “spontaneous abortion” represents by far the highest number in these reports. In other words, the FDA knew this vaccine would kill unborn babies, but they pushed it on pregnant women anyway.
All mRNA vaccines must be immediately halted, and FDA bureaucrats must be indicted and arrested
This confidential document — just the first of thousands yet to be released — reveals two critical things:
1) The FDA committed criminal fraud and misrepresentation in approving mRNA vaccines as “safe and effective.” This means top FDA decision makers must now face arrest and criminal prosecution.
2) The mRNA vaccine was known by Pfizer to be deadly even in its first three months of emergency use. This means Pfizer is also complicit in the continued deaths of innocent victims, as Pfizer itself should have pulled its deadly vaccine and halted all sales and distribution.
Find even more details in today’s Situation Update podcast which also covers Alex Baldwin’s magic gun, left-wing abortion pill gobblers protesting SCOTUS, Dr. Oz. running for the US Senate, Australia’s covid death camps and much more:
General Flynn warns of new lockdowns for new variants – world ID coming – being legislated in Australia
On the Alex Jones Show on Saturday, November 13th, former National Security Advisor General Michael T. Flynn issues an emergency warning to the world! That Warning has now come true. Look at what has happened in Australia. We are now one of the most maligned nations on earth thanks to all of our corrupt politicians infesting parliaments like cockroaches. Alex Jones has nailed it.
Tasmanian senator Jacqui Lambie terrorising the un-vaxxed and speaking against Pauline Hanson’s stop the mandate motion in the senate last week
While the Labor Premier and Health officials threaten the Far North over low vaccination rates homeless people too refuse the deadly jab
by Jim O’Toole in Cairns
Cairns health officials set up a makeshift Covid jab facility in a large city park frequented by homeless Aborigines and others to no avail as the disadvantaged people have woken up to the evil intent of Premier Annastacia Palaszczuk to have them inoculated with an experimental and proven, dangerous mRNA toxin containing foetal matter that will eventually kill.
The families of many tens of thousands of vaxx victims across the world and in Australia can attest to the deaths and injuries and the blinding fact the vaccine doesn’t prevent any coronavirus.
Even with the enticement of $25 a shot or free ice-creams not one of the poor people of Cairns and regions turned up to to get a jab.
The dopey and patronising Labor Party has not yet woken up that the bauble days of beads and King plates are long over.
Savvy Murris with IPhones have done their own research rather than listen to the lies of the politicians and health departments. Their research about the spiraling death and injury rate of vaxx victims has spread far and wide in Aboriginal communities.
Today a North Queensland Cowboys footballer is heading for the Aboriginal community of Palm Island near Townsville trying to coerce his indigenous relatives to get the jab.
Whatever his motives may be he will be wasting his time and further wrecking any notion of trust between government and Aborigines. Goodbye Reconciliation and good riddance!
The majority will never get the jab from these government liars and manipulators who have forever destroyed any hope of unity between black and white and let the unintelligent Premier at her peril take away their sit down money or any other of a multitude of taxpayer-funded benefits for refusing the jab.
The medical mafia and their dodgy data are wasted on our indigenous brothers.
Queensland Health Department is wasting its time trying to coerce Aborigines into getting the jab. Research by savvy Murris has revealed the ALP/LNP/Greens push for depopulation
Letter to the Editor
Moderna mRNA gene therapy has just been rubber stamped for use in Australia, is still an Experimental Test Vaccine in America under Emergency Protocol.:
Covid vaccine maker Moderna received 300,000 reports of side effects after vaccinations over a three-month period following the launch of its shot, according to an internal report from a company that helps Moderna manage the reports.
That figure is far higher than the number of side effect reports about Moderna’s vaccine publicly available in the federal system that tracks such adverse events.
Washington: In a first, a new study has pointed out that those taking the Moderna vaccine have reported more side effects than people who get the Pfizer/BioNTech jabs….
Vaccine manufacturers like Moderna are legally required to forward all side effect reports they receive to the Vaccine Adverse Events Reporting System, where they are made public each week.
Run by the Centers for Disease Control and Food & Drug Administration, the VAERS system is crucial to tracking potential problems with vaccines. It helped scientists determine the Covid vaccines may cause heart problems in young adults.
The reason for the gap is not clear. Moderna may simply still be processing the reports, though the number of reports about Moderna’s vaccine in VAERS from the first half of 2021 remained almost flat this week.
Moderna and IQVIA, the company that works with Moderna to handle the reports, did not return emails for comment.
The 300,000 figure comes from an internal update provided to employees by IQVIA, a little-known but enormous company that helps drugmakers manage clinical trials. Headquartered in North Carolina, IQVIA has 74,000 employees worldwide and had $11 billion in sales last year.
Earlier this week, Richard Staub, the president of IQVIA’s Research & Development Solutions division, sent a “Q2 2021 update” which was labeled “Confidential – For internal distribution only.”
A person with access to the presentation provided screenshots of the relevant slide, which clearly explains the 300,000 side effect reports were received over “a three-month span” – not since the introduction of the vaccine in December – and differentiates between them and “medical information queries.”
The slide does not make clear what three months are covered but refers to the “global launch” of the vaccine, which essentially took place in the first quarter of 2021. Whether the slide is referring to January through March or April through June, the 300,000 figure dwarfs the number of reports in VAERS for the Moderna vaccine for either period.
A query of VAERS this morning reveals roughly 110,500 adverse events reports worldwide for Spikevax completed from January through March. All but 650 were in the United States. VAERS also includes 78,000 reports completed from April through June, including 71,400 in the United States.
Those figures overstate the number of reports Moderna has provided, because they include many reports from patients, physicians, and other health-care providers, as well as those from Moderna.
VAERS was established in 1990 and is jointly managed by the CDC and FDA, which contract with General Dynamics to administer it. It has struggled to keep up with the hundreds of thousands of reports it has received about the Covid vaccines since their rollout began in December. For much of the spring, it lagged months behind in making reports public.
VAERS is usually characterized as a voluntary system. But physicians and healthcare providers are required to report certain serious post-vaccine side effects, including deaths. However, the CDC and FDA have no real way to check if they are doing so.
Healthcare providers do have discretion over whether they report less serious side effects. Many have decided not to do so for the Covid vaccines, because the volume of reports is already so high.
However, vaccine manufacturers must forward ALL reports they receive, as the VAERS Website makes clear. It distinguishes between healthcare providers, who are “strongly encouraged” to report various events, and manufacturers like Moderna, who “are required [emphasis added] to report to VAERS all adverse events that come to their attention.”
Moderna’s stock has nearly quadrupled this year as sales of the Covid vaccine have soared. On Thursday, the company reported $4.4 billion in sales and $2.8 billion in profits for the second quarter.
As of today’s update, VAERS contains more than “3,000 reports of deaths” following Moderna vaccinations.
from Alex Berenson, NSW
The active substance in each dose is 0.10 mg mRNA encoding the pre-fusion stabilized Spike glycoprotein of SARS-CoV-2 embedded in lipid nanoparticles. It also contains polyethylene glycol/macrogol (PEG) as part of PEG2000-DMG and is a multidose vial which contains 10 doses of 0.5 mL.
Other ingredients listed include:
- Lipid SM-102, cholesterol
- 1,2-distearoyl-sn-glycero-3-phosphocholine (DSPC)
- 1,2-Dimyristoyl-rac-glycero-3-methoxypolyethylene glycol-2000 (PEG2000-DMG)
- Trometamol (tris)
- Trometamol hydrochloride (tris HCl)
- Acetic acid
- Sodium acetate trihydrate
- Water for injection
Uncommon side effects
Some of the more uncommon/rare or unknown side effects that may still occur include:
- Temporary one-sided facial drooping (Bell’s palsy)
- Swelling of the face (It should be noted that swelling of the face can occur in patients who have had facial cosmetic injections.)
- Severe allergic reactions (anaphylaxis)
from Open Access Government https://www.openaccessgovernment.org/what-are-the-side-effects-of-the-moderna-vaccine/106767/
First Postmortem Of Covid-Vaxxed Patient; Body Riddled With Viral RNA Published on June 17, 2021 Written by halturnerradioshow.com
The first-ever autopsy of a person vaccinated against COVID-19, who tested negative 18 days later upon hospital admission but at 24 days after the VAX, has revealed viral RNA was found in almost every organ of the body. The vaccine, while triggering an immune response, DID NOT STOP the virus from entering every organ in the body. The viral RNA was found in virtually every organ in the body, which means the spike proteins as well.
There are antibodies (like the “vaccine” is supposed to create) but they’re irrelevant because, based on a study from Japan, we now know that the spike S1 protein is what does the damage. We spoke to one Infectious Disease specialist from a hospital in New Jersey this morning. We sent the actual autopsy findings to him and asked for his thoughts. When he called back a while later, he was clearly shaken-up. He told us “You cannot quote me by name, I will get fired by the hospital if you do.” We agreed to conceal his identity.
He then told us: “People think that only a MINORITY of people get adverse effects from the vaccine. Based on this new research, it means that everyone – EVENTUALLY -will have adverse effects, because those spike proteins will be binding to ACE2 receptors everywhere in the body.
That mRNA was supposed to stay in the injection site and it’s not. That means the spike proteins created by the mRNA will be in every organ as well, and we now know it is the spike proteins that do the damage. Worse, the viral RNA being found in every organ despite a vaccine, indicates either: 1) The vaccine doesn’t work at all, OR; 2) The virus is enjoying Antibody Dependent Enhancement (ADE), meaning it actually spreads FASTER in vaccinated people. This is a GLOBAL TIMEBOMB.”
According to the published postmortem report, the vaccinated man was 86 years old and tested NEGATIVE for COVID-19 when first admitted to the hospital with severe gastro-intestinal trouble and difficulty breathing.
Here is what the reports describes: We report on an 86-year-old male resident of a retirement home who received vaccine against SARS-CoV-2.
Past medical history included systemic arterial hypertension, chronic venous insufficiency, dementia and prostate carcinoma. On January 9, 2021, the man received lipid nanoparticle-formulated, nucleoside-modified RNA vaccine BNT162b2 in a 30 µg dose. On that day and in the following 2 weeks, he presented with no clinical symptoms (Table 1). On day 18, he was admitted to hospital for worsening diarrhea. Since he did not present with any clinical signs of COVID-19, isolation in a specific setting did not occur. Laboratory testing revealed hypochromic anemia and increased creatinine serum levels. Antigen test and polymerase chain reaction (PCR) for SARS-CoV-2 were negative. The report of the postmortem makes clear tests showed “no morphological changes associated with COVID” in his organs. “ (Morphological” means structural.)
COVID infection is now known to cause very specific structural changes to the places it infects. THOSE CHANGES HAD NOT APPEARED in the vaccinated man before he died. The now dead vaccinated man was in a room where another patient ultimately tested POSTIVE for COVID, and the report states they think the dead vaccinated man caught COVID after he was admitted, from the other patient in the same room. So the damage to the organs of the now dead vaccine recipient, took place BEFORE he was infected with COVID by the other hospital room patient.
Worse, once the vaccinated man actually got COVID, it spread so fast within his body, he apparently never stood a chance.
URGENT REQUEST FOLLOWING RESEARCH SHOWING THE “S PROTEIN” IN THE PFIZER JAB IS A TOXIN
June 4, 2021
From: Sue Grey firstname.lastname@example.org
Date: Thu, 3 Jun 2021, 23:33
Subject: OPEN LETTER No 2- An URGENT REQUEST FOLLOWING RESEARCH SHOWING THE “S PROTEIN” IN THE PFIZER JAB IS A TOXIN
To: Rt Hon Jacinda Ardern email@example.com, Hon David Parker firstname.lastname@example.org, Hon Andrew Little email@example.com, Hon Chris Hipkins firstname.lastname@example.org, email@example.com, Chris James Chris.James@health.govt.nz, firstname.lastname@example.org
Dear Prime Minister, Attorney-General, Minister of Health, Minister of Covid, Minister or Seniors, Director General of Health and Chris Hipkins.
I attach below some new and very important research which I must assume your advisors have not yet provided to you, or the experimental Pfizer injection rollout would surely already have been suspended.
It is now clearly established that the SProtein is a toxin that causes the harmful symptoms known as “Covid”.
Lawyer and Microbiologist Sue Grey (below) warns PM Ardern of criminal charges should Covid jabs continue
I surely don’t need to explain the legal, ethical and human rights consequences of a government knowingly promoting a program which intentionally injects a life threatening toxin into healthy people.
I also attach a report indicating that injected nanoparticles (and the SProtein) do not remain in the arm muscle but instead circulate throughout the whole body.
The combined effect is that the Pfizer jab injects mRNA to take over cells to manufacture the deadly SProtein toxin and this spread throughout much of the body, manufacturing the SProtein toxin for days and in some cases many weeks.
This explains why even the limited available research from the two months of study as summarised in the Comirnaty Data Sheet identifies possible harm to many different parts of the body including the heart, blood, brain, musculoskeletal system, nervous system, fainting and dizziness etc.
This is no longer just a shocking experiment. Everyone involved is now on notice of this “injection roulette” which may result in death or serious injury to previously healthy people. The health and safety implications for employers and those who push this jab, are significant.
No post injection death can legitimately be ruled out as being caused or contributed by the injection, at least not without a full coroner’s report. Certainly any post vax stroke, heart attack, other blood disorder, nervous system disorder or even suicide or car accident (known overseas as “vaccidents”) must prima facie be assumed to be caused or contributed to by the jab, at least until a full coroners report is undertaken.
Similarly it is not good enough to claim that our seniors who die post jab were frail and likely to die. Surely if they were that frail they should have been spared from the jab. Anyway, surely “deaths post Jab” should be treated consistently with “deaths post Covid”.
Despite the secretive, flawed and very passive official post jab injury reporting process ( CARM), and as a result of the more active community led follow up, you are already on notice of a number of deaths and life threatening and life changing harm from this injection. The deaths and harm will inevitably continue if there are any further injections. Perhaps initially you had an excuse that you thought the SProtein was “safe”. However now you are on notice that it is not “safe” by any definition.
Further, although you in privileged position are on notice, many members of the public who you were elected to represent remain deceived by misleading claims in crown propaganda that the jab is “safe and effective”. In these circumstances there can be no “Informed consent”., Each jab without Informed consent is in breach of the Health and Disability Code and is an assault.
In these circumstances, the ongoing program is surely criminal, and indeed may result in Homicide as defined by the Crimes Act:
Homicide is the killing of a human being by another, directly or indirectly, by any means whatsoever.
Compare: 1908 No 32 s 173
Anyone who aids, abets or otherwise incites homicide is a party to that homicide.
I note that the Director-General of Health has shared his view in sworn evidence that Covid is the most serious health issue for New Zealand in 100 years.
I invite you all to consider that claim very carefully and critically. Please put Covid in perspective against the many other challenges which we face, including for example heart attacks, strokes, cancer, suicide accidents and diabetes and the nitrate and other contamination of much of our water.
Surely you must agree that the harm is not from “Covid” but from the “Response to Covid”.
The best expert evidence is that the risk from Covid is similar to the risk from influenza. Many experts are now saying that Covid is simply a rebranding of influenza and colds, supported by PCR testing that was never intended as a diagnostic tool. The WHO says that PCR testing should not be used beyond 20-25 cycles. OIA responses indicate that in NZ PCR tests use up to 45 cycles, which simply multiplies any contamination.
Our government is about to enter dangerous new phase if it proceeds to inject more healthy New Zealanders with an injection that experts have established is toxic.
Apart from the direct harm to those who choose, or are bullied to accept this injection, there is considerable peripheral harm. This includes the contamination of our Blood Bank with SProtein. We can only speculate on the risks for vulnerable people who receive blood contaminated with this toxin.
Please stop and reflect. Please listen to international experts who are independent from Big Pharma and who are not invested in the Covid paradigm.
Please listen to the New Zealand scientific and medical experts who have put their careers and reputations on the line out of extreme concern.
Please correct the misinformation that this injection is “safe and effective” and “approved by Medsafe” when in fact it did not meet the statutory criteria that “benefit exceeds risk”.
There is no imminent health risk from suspending the program. Dr Bloomfield’s sworn evidence was that the risks were mainly financial and reputational.
Please find the courage to challenge whoever is driving this, and any who act on dogma rather than evidence, reason or ethics.
The future of New Zealand depends on your courage to step up and make this critical call for our people.
I urge you to listen, engage and act in the public interest.
Please put aside your pride and the dogma, and suspend this program.
I am happy to assist however I can.
Sue Grey LLB (Hons), BSc (Biochemistry and Microbiology), RSHDipPHI
Co-leader NZ Outdoors Party email@example.com
Letter to the Editor
Hello fellow Australians,
Government responses to COVID 19 are often said to be “led by science.” However what we are seeing is the widespread censorship of science to support a narrative. It seems anything that challenges the orthodox view is ignored, banned or undermined. While this persists no government can claim their polices are “led by science.”
We contrast the statements about COVID 19 of four eminently qualified scientists. Dr Mike Yeadon, Sir Patrick Vallance, Chris Witty and Dr. Roger Hodkinson. All four should be heard but only two are. While Patrick Vallance and Chris Witty are given the maximum public exposure, Dr’s Yeadon and Hodkinson are almost completely ignored by the politicians and the mainstream media and heavily censored on social media.
Watch here to find out why:
Science invites critical debate. There is no such thing as unquestionable science. Every attempt by corporations and the politicians to limit freedom of speech, deny expert opinion, hide published science and censor all who highlight it, adds to the growing evidence that their policies are utterly divorced from science.
May you find peace, ease, and well being,
from Courier Mail
A defiant Gold Coast hairdresser is standing by her decision to ban COVID-vaccinated customers from her salon, despite being slammed by experts and social media critics.
Yazmina Adler (below), owner of the Khemia HI Vibe Frequency Salon at Palm Beach, unleashed a storm of controversy when she announced on Instagram this week that clients who had received the jab were not welcome in her shop because of the vaccine’s ‘unknown health effects’ and reputed ‘unusual signs and symptoms within the menstrual cycle’.
The decision was slammed as ‘ill-informed to the point of being dangerous and irresponsible’ by Dr Bruce Willett, Queensland chair of the Royal Australian College of General Practitioners.
While other health experts labelled it as “absurd, ridiculous and causing a public health risk”, and Dr Sonu Haikerwal, of the Upper Coomera Respiratory Clinic and Haan Health called it a “slap in the face to the health workers who’ve ensured the community remains free of COVID-19”.
But Ms Adler, 30, who has been a hairdresser since before leaving school at 15, told The Courier-Mail on Thursday she was ‘standing by my convictions’.
She said that while she had copped plenty of abuse – forcing her to remove her business address online and screen calls – she had also received ‘thousands’ of messages of support.
“It’s intense, people (critics) are going hard, but it takes a lot of courage to stand up against the so-called norm,” she said.
“It (concern about the vaccine) is out there and all I’ve done is brought it to the surface. There are many people that I know of that feel the same way.
“This is a very controversial topic so it’s going to draw out a lot of haters, but the support is outweighing the criticism 100 per cent.”
Brainless Australians lining up for Covid mRNA gene therapy shot
Open letter to Minister Greg Hunt from Australian Vaccination Network
The Honourable Greg Hunt MP
Federal Minister for Health and Ageing
PO Box 647
Somerville, Vic 3912
May 30, 2021
Dear Mr Hunt,
On behalf of the tens of thousands of members and supporters of The Australian Vaccination-risks Network (AVN), we are writing to you with the many concerns we have around the COVID-19 vaccination roll-out. We demand, based on the precautionary principle, that the current mRNA and viral vector vaccination experimental trial be immediately halted until independent scientific safety and efficacy evaluations can be unequivocally established. We understand that Queensland has, as of 21st May 2021, abandoned the AstraZeneca viral vector vaccination program due to injuries and deaths following vaccination.
We are very concerned that the COVID-19 vaccines have only been given provisional approval by the TGA under the State of Emergency declaration and that the decision to vaccinate the Australian public has been made on the basis of short term efficacy and safety data. It has been conceded by the TGA and AHPRA that there is no longitudinal scientific data relating to risk/benefit profile. Why is our government coercing Australians to have experimental injections which have been developed, marketed and distributed in less than a year while previous vaccine development took between 10-15 years?
In an interview on Insiders you stated:
“The world is engaged in the largest clinical trial, the largest global vaccination trial ever, and we will have enormous amounts of data.”
As you have publicly admitted, these injections are still in clinical trials, and anyone who gets the shot is now part of an experiment.
Why haven’t you given instructions to health professionals to inform every person receiving the shot that they are participating in an experiment? Informed consent is essential for any medical procedure as per the Australian Immunisation Handbook and the Nuremberg Code.
These Covid vaccines are not necessary. According to the CDC’s current best estimate, “the infection fatality rate” (IFR) for Covid-19 is less than 1 percent for people aged 69 and younger. Vaccine manufacturers claim that COVID-19 vaccines are 95 percent “effective,” but the FDA is allowing companies to define effectiveness as “prevention of mild symptoms.” The studies are not designed to detect a reduction in outcomes such as severe illness, hospitalization or death. For individuals who develop severe symptoms, the vaccine is not a remedy. Instead, nutritional and oxidative support can help keep the illness from going into “overdrive.” Peter Doshi from the British Medical Journal has concerns that the current trials are not designed to show whether the injections will save any lives. In fact, reports since the commencement of the rollout in countries around the world are showing the vaccines are causing deaths and injuries.
Participants in every COVID-19 vaccine trial reported adverse reactions including high fever, chills, muscle pains and headaches. Some even reported severe reactions that required hospitalization and invasive treatment. According to the FDA, potential long-term effects may include Guillain-Barré syndrome, brain swelling, muscle weakness and paralysis, convulsions and seizures, stroke, narcolepsy, thrombosis with thrombocytopenia syndrome (TTS), shock, heart attack, autoimmune disease, arthritis and joint pain, multisystem inflammatory syndrome in children, and death.
Some UK health workers have experienced anaphylactic shock after receiving one dose of the approved vaccine and the UK government has warned those with severe allergies to avoid the Pfizer injection. Manufacturers have been granted complete indemnity, freedom from liability even though all previous attempts at creating coronavirus vaccines caused harm and never advanced to regulatory approval.
Sadly, we are seeing the devastating results of these government-sponsored and unnecessary, untested experimental injections on people all over the world. As of May 14, 2021, the number of reported US deaths following COVID-19 vaccines was 4,201 according to data released today by the Centers for Disease Control and Prevention (CDC). The data comes directly from reports submitted to the Vaccine Adverse Event Reporting System (VAERS). A US Harvard Study concluded that “fewer than 1% of injuries were reported” to the database. Every week, VAERS makes public all vaccine injury reports received as of a specified date, usually about a week prior to the release date.
Between December 14, 2020 and May 14, 2021 there have been a total of 227,805 adverse events, including 4,201 deaths. This is alarming but not surprising as there is no data to suggest safety for the following groups of people: Anyone younger than age 18 or older than age 55, pregnant or lactating mothers, those with autoimmune conditions and immunocompromised individuals. The safety for other age groups is inconclusive as the clinical trial for Pfizer, and AstraZeneca will not conclude until 2023.
In Australia, the reported adverse events were over 19,598 on May 20, 2021 according to the report on the TGA website. We are also hearing that thousands of women around the world are reporting disrupted menstrual cycles after receiving the COVID-19 vaccines. The U.K.’s government vaccine adverse event reporting system has collected more than 2,200 instances of reproductive disorders after coronavirus injections, including excessive or absent menstrual bleeding, delayed menstruation, vaginal haemorrhaging, miscarriages, and stillbirths.
Two prominent doctors, including the ex-head of Pfizer’s respiratory research, had warned that Covid-19 vaccines contain a spike protein called syncytin-1, vital for the formation of the placenta. If the vaccine triggers an immune response to this protein, then female infertility, miscarriage or birth defects could result.
On Monday 22 February 2021, COVID-19 vaccinations began in Australia. By May 12, the TGA had received 6 reports of Guillain-Barre Syndrome (GBS) following the injection of the AstraZeneca COVID-19 vaccine. There have also been reports to the TGA of 18 cases of Thrombosis with thrombocytopenia syndrome (TTS), a devastating condition that leaves the patient with low platelet levels and a tendency to bleed at the same time, and which has a fatality rate of 25%. Reports as at May 2 show that there are approximately 20 cases of anaphylaxis reported in Australia per million doses of the Comirnaty vaccine. How many reactions to vaccination are actually reported to the TGA’s database of adverse reactions? Do frontline medical staff know that they can and should report a suspected adverse event following a vaccination? We know that according to the study performed by Harvard less than 1% of all adverse reactions are submitted to VAERS, so we can only assume (as no such study has been performed by the Australian government) that the percentage would be similar in Australia.
Informed consent is being bypassed. According to the Australian Immunisation Handbook on the TGA website, informed consent is essential. It states:
Valid consent is the voluntary agreement by an individual to a proposed procedure, which is given after sufficient, appropriate and reliable information about the procedure, including the potential risks and benefits, has been conveyed to that individual and it must be given voluntarily in the absence of undue pressure, coercion or manipulation.
According to the Royal Australian College of General Practitioners:
Informed consent is the process whereby a patient makes a voluntary decision about their medical care with knowledge and understanding of the benefits and potential risks involved. A patient should only agree to the proposed treatment if he or she has been provided with sufficient information including the benefits, associated risks and alternative management options, so they are able to make an appropriate decision about their own health care.
Clearly, we are not able to make an informed choice unless we have the full information to do so. This clinical trial we are engaged in does not meet the requirements of full disclosure and so this vaccination program must cease immediately. Many Australians are being coerced and pressured into taking the vaccine against their will due to the ongoing discussions by the Australian government around restrictions being imposed on those who do not consent to the Covid-19 vaccine. This goes against the values of Australia as a free country where the citizens are entitled to make their own informed medical decisions.
We look forward to receiving a written reply to our concerns and we request urgent action in response to the above information, ensuring a halt to the rollout of the COVID-19 vaccines for the safety of all Australians.
Ms Meryl Dorey
President, Australian Vaccine-risks Network (AVN)
On behalf of the Members of the AVN and our supporters
Cc:/The Hon Mark Butler MP, Shadow Minister for Health and Ageing
Letter to the Editor
I had COVID for one day on June 26, 2020. My doctor prescribed Hydroxycholoroquine, Zinc, Vitamin D3, Chlorella, Collagen, Damiana Leaf Extract, and Astralagus, and I tested NEGATIVE within 24 hours. But my doctor was actually sane.
On the other hand, the Lethal Injection results in the following adverse events:
1. Known injury and deaths from Messenger RNA prions, which in the case of cattle, results in “Mad Cow Disease,” and in the case of human beings, results in the manifestation of brain dysfunction and hysteria;
2. Known injury and death from anaphylactic shock resulting from the infusion of Messenger RNA through the vaccine;
3. Known injury and death from toxic lung, heart, and brain paralysis resulting from the infusion of Messenger RNA through the vaccine;
4. Known injury and death from toxic blood clotting resulting from the infusion of Messenger RNA through the vaccine; and:
5. Known injury and death from toxemia arising from infertility complications resulting from the infusion of Messenger RNA through the vaccine.
6. Known injury and death from mitochondrial cancer from lipid nanoparticles causing cytokine storms of spike proteins which deprive the heart, lungs, and brain of oxygen.
7. A phenomenon known as Frequency Transmissibility Shedding caused by 5G Electromagnetic Transmission Nanoparticles which cause UNVACCINATED people to be harmed if they are in direct proximity with VACCINATED people; and:
8. THERE IS NO CURE for the Experimental Use Authorization Injection. 80% will die within the first five years, and 100% will all die within ten years, due to the replication and proliferation of oxygen-depriving spike proteins.
So what choice makes more sense for your survival, I ask respectfully?
from Steven Fishman